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Links from GEO DataSets

Items: 19

1.

Analysing of Chromosome VIII of EC9-7 after experimental evolution (S. cerevisiae)

(Submitter supplied) The genomic DNA of wild-type chromosome VIII of evolved EC9-7 cells was extracted from the gel of pulsed field gel electrophoresis (PFGE), and analyzed by array-CGH to identify its chromosomal composition
Organism:
Saccharomyces cerevisiae
Type:
Genome variation profiling by array
Platform:
GPL13701
2 Samples
Download data: GPR
Series
Accession:
GSE33652
ID:
200033652
2.

Analysis of Chromosome VIII of EC-C1 strains (S. cerevisiae)

(Submitter supplied) The genomic DNA of rearranged chromosome VIII (~900kb) of EC9 diploid strain was extracted from the gel of pulsed field gel electrophoresis (PFGE), and analyzed by array-CGH to identify it's amplified regions
Organism:
Saccharomyces cerevisiae
Type:
Genome variation profiling by array
Platform:
GPL7305
1 Sample
Download data: GPR
Series
Accession:
GSE38034
ID:
200038034
3.

The expression profile under cooper sulfate treatment

(Submitter supplied) The expression profile of natural isolate of S. cerevisiae carrying different copy of CUP2 were compared under cooper sulfate stress
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL13701
11 Samples
Download data: GPR
Series
Accession:
GSE31661
ID:
200031661
4.

Characterization of chromosome rearrangement of EC strain (S. cerevisiae)

(Submitter supplied) The EC strain karyotype was analyzed by array-CGH to identify amplified chromosomal regions.
Organism:
Saccharomyces cerevisiae
Type:
Genome variation profiling by array
Platform:
GPL7305
3 Samples
Download data: GPR
Series
Accession:
GSE22431
ID:
200022431
5.

Characteristic genome rearrangements in experimental evolution

(Submitter supplied) Genome rearrangements, especially amplifications and deletions, have regularly been observed as responses to sustained application of the same strong selective pressure in microbial populations growing in continuous culture. We studied eight strains of budding yeast (Saccharomyces cerevisiae) isolated after 100–500 generations of growth in glucose-limited chemostats. Changes in DNA copy number were assessed at single-gene resolution by using DNA microarray-based comparative genomic hybridization. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome variation profiling by array
Platforms:
GPL2836 GPL2636 GPL2835
45 Samples
Download data
Series
Accession:
GSE3285
ID:
200003285
6.

Copper regulon in S. cerevisiae

(Submitter supplied) In Saccharomyces cerevisiae, copper ions regulate gene expression through the two transcriptional activators, Ace1 and Mac1. Ace1 mediates Cu-induced gene expression in cells exposed to stressful levels of copper salts, whereas Mac1 activates a subset of genes under copper-deficient conditions. DNA microarray hybridization experiments revealed a limited set of yeast genes differentially expressed under growth conditions of excess copper or copper deficiency. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Dataset:
GDS69
Platform:
GPL65
6 Samples
Download data
Series
Accession:
GSE26
ID:
200000026
7.
Full record GDS69

Copper regulon

Differential gene expression under growth conditions of excess copper or copper deficiency, regulated by Mac1 or Ace1 transcriptional activators.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, log ratio, 3 protocol sets
Platform:
GPL65
Series:
GSE26
6 Samples
Download data
DataSet
Accession:
GDS69
ID:
69
8.

Role of 14-3-3 in the transcriptional response of Saccharomyces cerevisiae to potassium starvation.

(Submitter supplied) We investigated the transcriptional response of yeast Saccharomyces cerevisiae bmh1 and bmh2 deletion mutants to potassium starvation. To this end yeast strains were grown for 60 min in media without potassium or in media with a standard potassium concentration (50 mM KCl). Using Serial Analysis of Gene Expression (SAGE)-tag sequencing the effect of potassium starvation on the transcriptome was determined. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13821
12 Samples
Download data: XLSX
Series
Accession:
GSE85564
ID:
200085564
9.

Transcriptional response of Saccharomyces cerevisiae to potassium starvation

(Submitter supplied) In this study we investigated the transcriptional response of the yeast Saccharomyces cerevisiae to potassium starvation. To this end yeast cells were grown for 60 min in media without potassium or in media with a standard potassium concnetration (50 mM KCl). Using Serial Analysis of Gene Expression (SAGE)-tag sequencing the effect of potassium starvation on the transcriptome was determined.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13821
8 Samples
Download data: TXT
Series
Accession:
GSE57093
ID:
200057093
10.

Transcription-induced formation of extrachromosomal DNA during yeast ageing

(Submitter supplied) Extrachromosomal circular DNA (eccDNA) facilitates adaptive evolution by allowing rapid and extensive gene copy number variation, and is implicated in the pathology of cancer and ageing. Here, we demonstrate that yeast aged under environmental copper accumulate high levels of eccDNA containing the copper resistance gene CUP1. Transcription of CUP1 causes CUP1 eccDNA accumulation, which occurs in the absence of phenotypic selection. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL17342
30 Samples
Download data: TXT
Series
Accession:
GSE135542
ID:
200135542
11.

The transient inactivation of the master cell cycle phosphatase Cdc14 causes genomic instability in diploid cells of Saccharomyces cerevisiae.

(Submitter supplied) Genomic instability is a common feature found in cancer cells. Accordingly, many tumor suppressor genes identified in familiar cancer syndromes are involved in the maintenance of the stability of the genome during every cell division, and are commonly referred to as caretakers. Inactivating mutations and epigenetic silencing of caretakers are thought to be the most important mechanism that explains cancer-related genome instability. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome variation profiling by SNP array
Platform:
GPL20143
28 Samples
Download data: GPR, XLSX
Series
Accession:
GSE68530
ID:
200068530
12.

Rap1 and Abf1 DNA-binding ts mutants and wild type after 1 hr at 37 C

(Submitter supplied) Abf1 and Rap1 are General Regulatory Factors that contribute to transcriptional activation of a large number of genes, as well as to replication, silencing, and telomere structure in yeast. In spite of their widespread roles in transcription, the scope of their functional targets genome-wide has not been previously determined. We have used microarrays to examine the contribution of these essential GRFs to transcription genome-wide, by using ts mutants that dissociate from their binding sites at 37 C. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Datasets:
GDS2533 GDS3198
Platform:
GPL90
12 Samples
Download data: CEL
Series
Accession:
GSE6073
ID:
200006073
13.
Full record GDS3198

Abf1 DNA-binding mutant

Analysis of temperature sensitive Abf1 mutant cells subjected to a temperature of 37 degrees C to dissociate the mutant protein from its DNA binding sites. Results provide insight into the contribution of this general regulatory factor to transcription genome-wide.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL90
Series:
GSE6073
6 Samples
Download data: CEL
14.
Full record GDS2533

Rap1 DNA-binding mutant

Analysis of temperature sensitive Rap1 mutant cells subjected to a temperature of 37 degrees C to dissociate the mutant protein from its DNA binding sites. Results provide insight into the contribution of this general regulatory factor to transcription genome-wide.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL90
Series:
GSE6073
6 Samples
Download data: CEL
15.

Expression data from S. cerevisiae after evolution under diverse conditions

(Submitter supplied) We conducted a set of lab-evolution experiments in yeast and followed the long-term dynamics of aneuploidy under diverse conditions including heat shock and high PH.
Organism:
Saccharomyces cerevisiae; Schizosaccharomyces pombe
Type:
Expression profiling by array
Platform:
GPL2529
40 Samples
Download data: CEL
Series
Accession:
GSE40817
ID:
200040817
16.

Expression analysis of genetically enginering S. cerevisiae strains

(Submitter supplied) Transcriptomes of transgenic strains and of evolved mutants bearing the macrotene chromosomes
Organism:
Saccharomyces cerevisiae; Saccharomyces cerevisiae S288C
Type:
Expression profiling by array
Platform:
GPL19506
4 Samples
Download data: GPR, TXT
Series
Accession:
GSE64431
ID:
200064431
17.

Natural variation in the consequences of gene overexpression during osmotic stress

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL17342 GPL21656
59 Samples
Download data
Series
Accession:
GSE226248
ID:
200226248
18.

Natural variation in the consequences of gene overexpression during osmotic stress [BAR-Seq]

(Submitter supplied) Free-living cells live in fluctuating environments and must be able to respond rapidly in order to survive. Genetic background can influence how an individual responds to a changing environment, including stressful changes. Changes in gene copy number can influence stress tolerance and responses, presumably due to corresponding changes in gene expression. However, we recently showed that strains vary in their ability to tolerate gene copy number differences; how this influences variation in stress tolerance is relatively unknown. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL21656
24 Samples
Download data: TXT
Series
Accession:
GSE226247
ID:
200226247
19.

Natural variation in the consequences of gene overexpression during osmotic stress [RNA-Seq]

(Submitter supplied) We used RNA-Seq to measure transcript abundance in 4 Saccharomyces cerevisiae strains (BY4743, BC187, NCYC3290, and YPS128) from a diverse range of genetic lineages when growing in rich media (YPD) with 0.7M NaCl to characterize differential expression across strains in response to osmotic and ionic stress.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17342
35 Samples
Download data: TXT
Series
Accession:
GSE226246
ID:
200226246
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